Canonical Allele Identifier: CA1096534822

Gene: SLC22A3

Linked Data

• dbSNP Id: rs1787631222
• gnomAD v3: 6-160419235-TAATGAGC-T
• gnomAD v4: 6-160419235-TAATGAGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160419237_160419243del , CM000668.2:g.160419237_160419243del	GRCh38
NC_000006.11:g.160840269_160840275del , CM000668.1:g.160840269_160840275del	GRCh37
NC_000006.10:g.160760259_160760265del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000275300.3:c.975+8391_975+8397del MANE Select	ENSP00000275300.2:n.975+8391_975+8397del
ENST00000275300.2:c.975+8391_975+8397del	ENSP00000275300.2:n.975+8391_975+8397del
NM_021977.3:c.975+8391_975+8397del	NP_068812.1:n.975+8391_975+8397del
XM_005267106.3:c.582+8391_582+8397del	XP_005267163.1:n.582+8391_582+8397del
XM_005267107.2:c.976-6614_976-6608del	XP_005267164.1:n.976-6614_976-6608del
XM_011536075.1:c.519+8391_519+8397del	XP_011534377.1:n.519+8391_519+8397del
XM_011536076.1:c.519+8391_519+8397del	XP_011534378.1:n.519+8391_519+8397del
XM_011536077.1:c.519+8391_519+8397del	XP_011534379.1:n.519+8391_519+8397del
XM_011536078.1:c.975+8391_975+8397del	XP_011534380.1:n.975+8391_975+8397del
XR_245546.1:n.1017+8391_1017+8397del
XM_005267106.5:c.582+8391_582+8397del	XP_005267163.1:n.582+8391_582+8397del
XM_005267107.3:c.976-6614_976-6608del	XP_005267164.1:n.976-6614_976-6608del
XM_011536075.2:c.519+8391_519+8397del	XP_011534377.1:n.519+8391_519+8397del
XM_011536076.3:c.519+8391_519+8397del	XP_011534378.1:n.519+8391_519+8397del
XM_017011203.2:c.519+8391_519+8397del	XP_016866692.1:n.519+8391_519+8397del
XR_001743588.1:n.1017+8391_1017+8397del
XR_001743589.1:n.1017+8391_1017+8397del
NM_021977.4:c.975+8391_975+8397del MANE Select	NP_068812.1:n.975+8391_975+8397del